QAV Specialist

Dublin  ‐ Onsite
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Description

QAV Specialist
A global Biopharmaceutical leader is currently looking for a QAV Specialist to join their team on a new build project based in Ireland.
The responsibilities of the QAV Specialist will include:
  • Provide quality and cGMP input and oversight for all start-up project activities through commercial readiness and ongoing product disposition.
  • Provide QA support for risk based verification activities in the capacity of Quality Assurance Subject Matter Expert. Review and approval equipment/utilities verification documentation from design to post execution.
  • Participate in verification quality risk assessments and provide quality oversight to ensure verification quality risk assessments are effectively maintained/controlled.

The successful QAV Specialist will possess the below experience:
  • Min 5 years QA experience in a pharmaceutical manufacture/biopharmaceutical environment. (BDS experience is essential).
  • Must have strong process knowledge to include upstream and/or downstream processing.
  • An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.
  • Excellent communication & presentation skills are essential.

If you are interested in becoming a QAV Specialist, please apply.
Start date
ASAP
From
Quanta Consultancy Services
Published at
15.11.2017
Project ID:
1451882
Contract type
Freelance
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